Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Recalled by Zimmer Biomet, Inc. Due to Incorrect raw material used by the supplier in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Zimmer Biomet, Inc. directly.
Affected Products
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral Femoral Drill Guide Small
Quantity: 15
Why Was This Recalled?
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
Where Was This Sold?
This product was distributed to 7 states: CA, IN, LA, NM, NY, TX, WI
About Zimmer Biomet, Inc.
Zimmer Biomet, Inc. has 875 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report